Potential Genes and Mechanisms Linking Intracerebral Hemorrhage and Depression: A Bioinformatics-Based Study
Received 20 January 2021
Accepted for publication 17 March 2021
Published 7 April 2021 Volume 2021:14 Pages 1213—1226
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Scott Fraser
Cuihua Zou,1,2,* Xiaohua Huang,1,2,* Xuequn Lan,1 Xiaorui Huang,1 Yun Feng,1 Jianmin Huang,1 Lanqing Meng,1 Chongdong Jian,1 Donghua Zou,3 Jie Wang,4 Xuebin Li1,2
1Department of Neurology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, People’s Republic of China; 2Department of Neurology, Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, People’s Republic of China; 3Department of Neurology, The Fifth Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, 530022, People’s Republic of China; 4Department of Nephrology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, 533000, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Jie Wang; Xuebin Li
The Affiliated Hospital of Youjiang Medical University for Nationalities, 18 Zhongshan er Road, Baise, Guangxi, 533000, People’s Republic of China
Email [email protected]; [email protected]
Purpose: The purpose of this study was to investigate the potential pathogenic mechanisms of post-intracerebral hemorrhage depression.
Methods: Profiles of gene expression in brain tissue of patients with intracerebral hemorrhage (ICH) or depression were downloaded from the Gene Expression Omnibus (GEO) database. We analyzed differentially expressed genes (DEGs) for the two diseases separately. With these DEGs, we conducted an enrichment analysis based on Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) as well as cross-talk analysis, then we identified hub bridge genes using integrated bridge landscape analysis.
Results: We found 131 DEGs for interaction between ICH and depression. In the enrichment analysis, we found 55 GO terms and KEGG pathways involving interacting genes of ICH and depression, and 10 GO terms and 10 KEGG pathways most significantly related to cross-talk between ICH and depression. In the integrated bridge landscape analysis, we identified 20 hub bridge genes. In further analysis, we found that hub bridge genes HLA-A, HMOX1, and JUN related to endocytosis, cell adhesion, and phagosomes may exert their effects through the dopamine (DA) system and the serotonergic pathway post-ICH depression. HLA-A may play a role in the occurrence and development of ICH and depression through immune mediation and cell adhesion. HMOX1 and JUN may participate in the mechanism by interacting with HLA-A.
Conclusion: Through bioinformatics analysis, we identified potential hub bridge genes and pathways related to post-ICH depression. Our study provides references for further research on mechanisms on the pathogenesis of post-ICH depression.
Keywords: intracerebral hemorrhage, depression, differentially expressed genes, hub bridge genes
The global population is aging, and the prevalence and mortality of stroke are on the rise. According to the Global Burden of Disease Study 2016, the highest age-standardized incidences of stroke are observed in eastern Asia, especially in China, where incidence is 354 cases [95% confidence interval (CI) 331–378] per 100,000 person-years.1 In particular, ischemic stroke and hemorrhagic stroke accounted for about 70% and 28% of all stroke cases in China, respectively.2
Many survivors of stroke suffer from mental and cognitive disorders.3 Post-stroke depression (PSD), often occurring 3–6 months after stroke, is one of the most common mental disorders.4 PSD seriously affects the recovery of neurological function in stroke patients and increases the incidence of disability and mortality.5,6 The incidence of PSD in stroke survivors is 33%7 and the pathogenesis of PSD is complex. At present, research on the mechanisms of PSD has focused on depression after ischemic stroke and has neglected depression after hemorrhagic stroke.
Intracerebral hemorrhage (ICH) is a serious type of stroke, and it is associated with the highest mortality among all stroke types.8 According to the Framingham Heart Study in the USA, the incidence of ICH was 43 cases per 100,000 person-years in the period 1948–2016. An age-stratified analysis indicated a continued increase in ICH incidence among patients 75 years and older, with incidence reaching 176 cases per 100,000 person-years in the period 2000–2016.9 The pathogenesis of ICH is not completely clear, although studies have implicated miR-126, cerebral cavernous malformation (CCM) proteins, Ang-1/Tie2, Smad4, Notch3, lipocalin-2, and 1q22.10–17
Post-ICH depression is common, affecting around 20% of ICH survivors, and it is associated with late exacerbation of ICH.6,18 In addition, ICH is often accompanied by neurological dysfunction such as aphasia and related language disorders, and cognitive difficulties. These complications often mask depressive symptoms, making it difficult for physicians to diagnose depression and prescribe the appropriate treatment. Therefore, it is important to clarify the pathogenesis of post-ICH depression and find new prevention, diagnosis, and treatment methods. Studies have implicated inflammation, oxidative stress, apoptosis, and autophagy.19 However, the mechanisms of post-ICH depression are not fully understood.
There is a bi-directional relationship between stroke and depression, and some common mechanisms and risk genes between the two diseases have been identified.4 However, we are unaware of comprehensive, unbiased, integrated bioinformatics analysis of the mechanisms linking ICH and depression. In this study, we performed such an analysis to investigate the potential genes and mechanisms linking ICH and depression in order to provide a new theoretical basis for revealing the mechanisms behind the pathogenesis of post-ICH depression.
Materials and Methods
Data Collection and Processing
This study was based on Gene Expression Omnibus (GEO) datasets from post-mortem patients (www.ncbi.nlm.nih.gov/geo/). We included one dataset of ICH and seven datasets of depression: GSE24265 [11 brain specimens of ICH, including 4 perihematomal (PH) areas, PH areas suspected to present edema identified by neuroradiology images from 4 deceased patients who had a supratentorial intracerebral hemorrhage, 4 contralateral gray (CG) matter, and 3 contralateral white (CW) matter], GSE87610 [76 brain specimens of dorsolateral prefrontal cortex (DLPFC) from patients with depression], GSE92538 [76 brain samples of DLPFC from patients with depression], GSE54562 [10 brain samples of anterior cingulate cortex (ACC) from patients with depression], GSE54572 [12 brain samples of ACC from patients with depression], GSE54565 [16 brain samples of ACC from patients with depression], GSE54564 [21 brain samples of amygdala (AMY) from patients with depression], and GSE24095 [15 brain specimens of the hippocampus dentate gyrus (DG) and 15 brain specimens of the hippocampus CA1 subregion from patients with depression]. The data are summarized in Table 1.
Table 1 Data Collection
GSE54572 and GSE54565 datasets were based on the GPL570 Affymetrix Human Genome U133 Plus 2.0 Array platform (Affymetrix; Thermo Fisher Scientific, Waltham, MA, USA) and were combined to remove different batches. The GSE92538 dataset was based on the GPL10526 Affymetrix GeneChip Human Genome HG-U133 Plus 2 Array platform (Affymetrix; Thermo Fisher Scientific), and the GPL17027 dataset was based on the Affymetrix Human Genome U133A Array platform (Affymetrix; Thermo Fisher Scientific). These datasets were divided into batches. We used the “normalizeBetweenArrays” function of the limma package20 in R to standardize the data. If a gene had two or more expression values, we used the average as the gene expression value.
Principal Component Analysis and Screening for Differentially Expressed Genes
Principal component analysis (PCA) was performed using the FactoMineR (https://www.r-project.org/) and factoextra (https://github.com/cran/factoextra) packages in R to evaluate the data in each dataset.
The data were preprocessed and then screened to identify differentially expressed genes (DEGs) using the unpaired t-test provided by the limma package in R. The threshold of significance was defined as P < 0.01 in the dataset of ICH. Gene expression patterns were compared between PH and contralateral healthy tissue from the same individuals. To exclude inherent differences between white matter and grey matter not influenced by ICH, both white and grey matter from the contralateral hemisphere were independently compared against the PH tissue, then white and grey matter from the contralateral hemisphere were compared with each other. Therefore, three comparisons of gene expression were calculated per individual: PH vs CG, PH vs CW, and CW vs CG. DEGs in ICH were defined as intersection genes for the comparisons PH vs CG and PH vs CW that showed consistent expression, minus the DEGs from the comparison CG vs CW.
For the depression DEGs, we used the same tissue in the dataset and selected the DEGs that showed consistent up- or down-regulation and that fell within the top 100 Pi values, where [Pi = -lg (p)* |logFC|], p is p-value and FC is fold chang. Values for genes present in multiple datasets were defined as the sum of the values across the datasets. Two-way hierarchical clustering was performed on the DEG profiles of ICH based on Euclidean distance using pheatmap (https://github.com/cran/pheatmap).
Analysis of Functional Enrichment
We used the clusterProfiler21 package to examine DEGs of ICH and depression based on enrichment of Gene Ontology (GO) functions and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. We screened biological process GO terms and KEGG pathways that might be related to ICH and depression using Gene Set Enrichment Analysis (GSEA) (GSEA2-2.2.4, Java version).22 The datasets c5.bp.v6.2.symbols.gmt and c2.cp.kegg.v6.2.symbols.gmt in the MsigDB V6.2 database23 were used as reference gene sets, and GSEA was performed according to default parameters. We set nominal P < 0.05 as the threshold for significant enrichment.
DEGs of ICH and depression were divided into six modules: the ICH DEGs were one module, while the DEGs of the five tissues for depression were five modules. Based on the STRING database (version 11.0, https://string-db.org/)24, 131 interactions of ICH and depression were extracted from the cross-talk analysis. In the STRING database, the combined score was computed by combining the probabilities from the different evidence channels and corrected for the probability of randomly observing an interaction. The combined score of human proteins ranked 150 to 999 in the database. Only the interactions with combined scores > 700 were included in the present study. The Sankey (https://github.com/cran/sankey) diagram was used to demonstrate the functions and pathways of the interacting genes involved in ICH and depression.
Integrated Bridge Landscape Network and Hub Bridge Genes
Based on the cross-talk analysis, the bridge genes and their interaction pairs were analyzed in Cytoscape.25 The integrated bridge driving force was calculated as W = F * Pi *degree, where F is the driving force of bridge genes and degree represents the connectivity in the cross-talk network. The top 20 genes with the highest W values were defined as hub bridge genes. The GOSemSim26 package was used to calculate the driving force F of the function of the bridge genes, and the expression of bridge genes was explored, where expression was defined as the log2 value of the standardized expression.
Principal Component Analysis
The flowchart of this study is shown in Figure 1. The results of the PCA showed that the first and second principal components (PCs) explained 13.2% (GSE87610)-67.4% (GSE24265) of the variance in different datasets (Figure 2). Although the variance explained by PC1-2 depended on the dataset, the gene expression pattern was able to distinguish ICH and depression patients from normal control samples. Therefore, these datasets were used to analyze and identify links between ICH and depression. However, there was a greater degree of admixture in some PCs, which indicated the need to perform feature selection rather than use all genes.
Figure 1 Study flowchart.
Abbreviations: ACC, anterior cingulate cortex; AMY, amygdala; CA1, hippocampus CA1 subregion; DG, hippocampus dentate gyrus; DLPFC, dorsolateral prefrontal cortex; ICH, intracerebral hemorrhage.
DEGs in ICH and Depression
We identified DEGs for ICH and depression in comparison with healthy controls. For depression, we found 64 up-regulated and 19 down-regulated genes in DLPFC samples (from GSE87610, GSE92538-GPL10526, and GSE92538-GPL17027 datasets), 27 up-regulated and 73 down-regulated genes in ACC samples (GSE54562 and GSE54572-GSE54565 datasets), 51 up-regulated and 49 down-regulated genes in AMY samples (GSE54564 dataset), 23 up-regulated and 77 down-regulated genes in CA1 subregions of the hippocampus (GSE24095 dataset), and 40 up-regulated and 60 down-regulated genes in the DG of the hippocampus (GSE24095 dataset) (Figure 3A). The DEGs of ICH and depression are summarized in Table 2.
Table 2 DEGs in ICH and Depression
We identified 113 DEGs in the PH tissue of ICH patients in the GSE24265 dataset, of which 82 genes were up-regulated and 31 were down-regulated (Figure 3B). We explored DEGs with consistently up-regulated and down-regulated expression in ACC and DLPFC tissue samples from patients with depression (Figure 3C). Cluster analysis showed that the expression patterns of the 113 DEGs were able to distinguish ICH from healthy control samples (Figure 3D).
GO Terms and KEGG Pathways Related to Post-ICH Depression
GO and KEGG enrichment analysis of DEGs in ICH and depression suggested that mechanisms of depression may be related to extracellular matrix (ECM)-receptor interactions and regulation of actin cytoskeleton (Figure 4A). ICH mechanisms appeared to be related to cell adhesion molecules (CAMs), endocytosis, and type 1 diabetes mellitus (Figure 4B). The enrichment analysis results were verified through GSEA. Figure 4C and Table S1 show 55 GO terms and KEGG pathways involving interacting genes of ICH and depression. The 55 GO terms and KEGG pathways were mainly related to inflammation, immunity, stress, apoptosis, and autophagy. These GO terms and KEGG pathways may be involved in the pathogenesis of post-ICH depression.
In order to find more genes involved in mechanistic links between ICH and depression, we divided the five parts of depressed brain tissues (DLPFC, ACC, AMY, CA1, DG) and ICH DEGs into six modules (one module for ICH, five modules for depression) and conducted cross-talk analysis. We identified 131 DEGs for the interaction (Figure 5A). DEGs for interaction in ICH and depression were considered to bridge the two conditions. DEGs for interaction corresponding to diseases and tissues were defined as bridge genes, and the interaction between molecules encoded by those genes was defined as a bridge interaction.
GO Terms and KEGG Pathways Related to Cross-Talk Genes
Figure 5B shows the most significant GO terms related to cross-talk genes between ICH and depression. These terms included response to hypoxia, response to nutrient levels, negative regulation of DNA binding, positive regulation of neurological system processes, neuronal death, synapse organization, autophagy, cellular iron ion homeostasis, intrinsic apoptotic signaling pathway, and regulation of apoptotic signaling pathways. The most significant KEGG pathways related to cross-talk genes between ICH and depression included CAMs, type I diabetes mellitus, cellular senescence, regulation of actin cytoskeleton, endocytosis, ECM−receptor interaction, phagosome, neurotrophin signaling pathway, ferroptosis, and the Toll−like receptor signaling pathway (Figure 5C).
Integrated Bridge Landscape Network and Hub Bridge Genes
Using bridge genes, the pathways in which bridge genes are involved and other related genes in the pathway were used to build a network, which was considered the post-ICH depression-related gene regulatory network (Figure 5D). Any of these bridge genes may interact with other genes in the network to regulate relevant functional pathways, and thus, may play a role in the pathogenesis of post-ICH depression. We integrated the network to compute the function driving force F (Figure 6) using the gene expression Pi value (taking the mean value across multiple datasets), defined as Pi=-lg(p)*|log2FC| (Figure 7A). The integrated bridge driving force W was W = F * Pi * degree (where “degree” means the degree of connectivity in the cross-talk network). The W values of bridge genes are reported in Table S6. The larger the W value, the more critical the nodes in the network. The top 20 gene nodes with the highest W values in the network, defined as hub bridge genes, were ACTL7A, RACGAP1, PRKAG1, CDH12, DYNLL2, VCAM1, SPHK1, GOLGA2, METRNL, KLRC1, JUN, ITGA2B, CDH5, TOLLIP, ANXA2, HLA-B, TAP2, ITGA5, HLA-A, and HMOX1 (Figure 7B and Table S6).
Figure 6 Results of functional driving forces of the bridge genes. Histograms of the genes with the greatest functional drive in each tissue. The x-axis represents a standardized score of gene functional driving force.
Post-ICH depression is a common complication of ICH that significantly affects prognosis. Thus, it is crucial to clarify the mechanisms of post-ICH depression for its prevention and management. In this study, we aimed to investigate hub bridge genes and potential pathways of post-ICH depression based on the interaction network between ICH and depression. We identified hub bridge genes of post-ICH depression from the analysis of DEGs for interaction in ICH and depression. We found 55 GO terms and KEGG pathways involving interacting genes of ICH and depression. In the GO and KEGG enrichment analysis of ICH and depression DEGs, we identified GO terms and pathways the most significant related to cross-talk. These hub bridge genes, functions and pathways may be related to post-ICH depression.
Previous studies found that activation of microglia after ICH leads to the production of proinflammatory cytokines, neuronal death, and structural deterioration.27 Activation of microglia and expression of proinflammatory cytokines are closely related to the pathogenesis of depression.28 Inflammatory cytokines such as hs-CRP, TNF-α, IL-1β, IL-6, IL-18, and IFN-γ reduce 5-hydroxytryptamine (5-HT), dopamine (DA), and norepinephrine signaling.29 The increased expression of inflammatory factors over-activates the hypothalamic-pituitary-adrenal (HPA) axis.30 The development of depression is closely related to imbalance of the HPA axis as well as signaling by 5-HT, DA, and norepinephrine.31,32
In addition, after secondary brain injury in ICH, many signaling pathways are activated, such as those related to inflammation, oxidative stress, autophagy and apoptosis. In particular, inflammation is related mainly to Toll-like receptors and signaling pathways dependent on NF-kB or PPAR-γ. Oxidative stress is related to nuclear factor erythroid-2 related factor 2, as well as the PI3K/Akt and MAPK/p38 pathways. Autophagy is related to the mTOR signaling cascade and the NF-kB-mediated signaling pathway, while apoptosis is related to the death receptor-mediated apoptosis pathway, caspase-independent pathways, and mitochondrial apoptosis pathway. Moreover, oxidative stress, neuroinflammation, apoptosis and autophagy interact, and these pathways can serve as a bridge between ICH and depression.19 The 55 GO terms and KEGG pathways involving interacting genes of ICH and depression, which obtained in the analysis also involved immunity, apoptosis, stress, autophagy, and inflammation. These results align with previous studies.
In our work, we identified ACTL7A, RACGAP1, PRKAG1, CDH12, DYNLL2, VCAM1, SPHK1, GOLGA2, METRNL, KLRC1, JUN, ITGA2B, CDH5, TOLLIP, ANXA2, HLA-B, TAP2, ITGA5, HLA-A, and HMOX1 as hub bridge genes between ICH and depression. The proteins encoded by these genes may be potential biomarkers for post-ICH depression.
Some of the hub bridge genes identified here have already been implicated in the pathophysiology of both ICH and depression. For example, AHNAK/p11/ANXA2 controls L-type voltage-gated calcium channels on the cell surface, which regulate neuronal activity induced by calcium signals and control depressive behaviors.33 In animal models, high levels of anti-ANXA2-antibodies can induce the accumulation of immunoglobulin G in the brain, which exerts an antidepressant effect.34 Polymorphisms of the ANXA2 gene are associated with stroke, and the encoded protein, annexin A2, is involved in the regulated generation of plasmin, the primary fibrinolytic protease regulating hemostasis and thrombosis.35
Several HLA haplotypes (such as A*24~B*07~DRB1*11, A*01~B*52~DRB1*15, A*24~B*35~DRB1*11 and A*02~B*51~DRB1*11) have been associated with an increased risk of stroke, while others (such as A*26~B*38~DRB1*11 and A*03~B*35~DRB1*04) have shown protective effects against stroke. HLA-B * 35, b * 52 may affect stroke risk by changing the function of arterial endothelial cells.36 Meanwhile, the HLA system is related to the risk of bipolar manic-depressive illness: HLA-B*08:01 may help protect against it,37 and antidepressant treatment has been associated with altered levels of HLA antigens A and B in patients with this disorder.38
Antidepressants such as imipramine and fluoxetine can induce the expression of genes related to neuroprotection, such as heme oxygenase-1 (HMOX1, HO-1).39 At the same time, heme-binding protein promotes the migration and differentiation of endothelial progenitor cells through the HMOX1 pathway, and promotes the formation of new blood vessels, thus protecting the integrity of the blood-brain barrier, synaptic plasticity, and neural function.40 In addition, the presence of hemoglobin at the focus of ICH aggravates brain injury. Binding globin binds to hemoglobin, prevents its oxidation, and participates in neurotoxicity. HMOX1 is involved in this process.41 In experimental models of spontaneous ICH, overexpression of HMOX1 in astrocytes after acute ICH mitigates the breakdown of the blood-brain barrier and short-term neurological deficits, exerts a neuroprotective effect, and improves outcomes.42
C-Jun N-terminal kinase (JNK) is a key mitogen-activated protein kinase43 and an important regulator of inflammation and stress responses, and its expression is closely related to the development of central nervous system diseases.44 In ICH, levels of phosphorylated JNK 3 and C-Jun are up-regulated, and JNK contributes to neuronal apoptosis.45 JNK also helps regulate the expression of pro-inflammatory cytokines, the phosphorylation of glucocorticoid receptors, and neuroinflammation-induced depression.44
Previous studies support the idea that our hub bridge genes may be involved in the physiological and pathological processes of both ICH and depression, making them likely drivers of post-ICH depression. In the cross-talk analysis, JUN, the hub bridge gene of depression, interacts with HLA-A and HMOX1, the hub bridge genes of ICH. Previous studies have shown that HMOX1, JUN, and HLA-A are involved in the pathological processes of both ICH and depression. In our analysis, we found that the three interacting genes HLA-A, HMOX1, and JUN may play a role in the mechanism of ICH and depression by regulating the pathways of cellular senescence, endocytosis, type I diabetes mellitus, CAMs, phagosome, ferroptosis, and neurotrophin signaling.
In further analysis, we found that HLA-A may interact with the other hub bridge genes, HLA-B, HLA-C, HLA-F, and HLA-G. These genes are involved in the regulation of endocytosis, CAMs, and phagosome pathways. This, together with the abnormal expression of other hub bridge genes in the pathway, such as HLA-DPB1, CDH5, VCAM1, and CADM1, may play a role in immune mediation and cell adhesion, and therefore, in the occurrence and development of ICH and depression (Figure 8).
Lesions in the DA system play a key role in the pathophysiology of depression. Reduction in the number of DA neurons is associated with the severity of depression. Epothilone B can protect DA neurons by enhancing microtubule stability, mitigating damage to DA neurons and reducing the depressive behavior of post-ICH depressive patients. Protecting DA neurons can help reduce risk of post-ICH depression.46 The migration of mesencephalic dopaminergic neurons from the subventricular zone to their final positions in the substantia nigra compacta, ventral tegmental area, and retrorubral field is controlled by signaling from neurotrophic factors, CAMs, and extracellular matrix molecules.47 Neural cell adhesion molecule (NCAM) is involved in the regulation of neurotransmitter DA receptor D(2)R transport and receptor-mediated signal transduction and behavior.48 DA acting on D2 receptor may regulate the structural plasticity of neurons and inhibit neurotransmission by changing the polysialylated form of NCAM expression.49 Maturation and NCAM-driven plasticity in dopaminergic brain areas can be affected by early life stress at different stages of ontogenesis and in a sex-specific manner.50 NCAM can mediate the survival of DA neurons through signaling pathways induced by mitogen-activated protein and ERK kinase, fibroblast growth factor receptor, protein kinase A, and protein kinase C.51 In addition, the phagocytic inflammatory response of microglia leads to the complement-mediated loss of dopaminergic neurons, leading to neurodegeneration.52 The early endocytic and endocytosis pathways play an important role in supporting rapid dopaminergic neurotransmission.53 Heptahelical G protein-coupled receptors (GPCRs) comprise the largest superfamily of signal transduction receptors, including adrenergic and dopaminergic receptors. Endocytic membrane transporter receptors to lysosomes play an important role in promoting down-regulation of GPCRs in some nerve cell types. Different GPCR endocytosis pathways may operate in parallel in the same cell, internalizing structurally homologous GPCR subtypes to different extents.54 Clarifying how GPCR signaling and membrane trafficking regulate specific subtypes of adrenergic and DA receptors could significantly advance the treatment of post-stroke depression. To summarize, DA system lesion plays a key role in the pathophysiology of post-ICH depression, and endocytosis, CAMs, and phagosome signaling may play an important role in this mechanism.
In addition, JUN, NCAM, and endocytosis play a role in 5-HT-related depression and antidepressant mechanisms. The human 5-HT(6) receptor [5-HT(6)R] interacts with Jun activation domain-binding protein-1 (Jab1). Jab1 provides a novel signal transduction pathway for 5-HT(6)R and may play an important role in 5-HT(6)R-mediated changes in the brain, including changes associated with depression.55 The G-allele of rs6295 is known to be associated with aspects of major depression, and the rs6295 G-/C-allelic variant is located in the promoter region of the human HTR1a gene, which encodes the G-protein-coupled receptor for 5-HT. C-Jun activates the rs6295 G-allelic variant.56 NCAM L1 may serve as a biomarker of response to selective serotonin reuptake inhibitors (SSRIs). The close homolog of L1 (CHL1) is a CAM involved in the regulation of neuronal survival and growth. Down-regulation of CHL1 in immune cells and brain tissue may be related to the immune pathogenesis of depression.57 The 5-HT1A receptor, a common GPCR associated with neuropsychiatric disorders such as depression, is an important drug target. The 5-HT1A receptor undergoes endocytosis mainly through the clathrin-mediated pathway and then circulates to the plasma membrane through the recycling endosome. The molecular mechanism of GPCR endocytosis may provide new insights into the potential mode of action of antidepressants acting through the serotonergic pathway.58
Although the present study provides new insights into the links between ICH and depression, it also contains several limitations. First, since brain specimens are very difficult to obtain, only 11 brain specimens of ICH were included in the present study. Second, we did not apply multiple testing correction in our statistical analyses. Third, our results are based on postmortem samples and so should be validated in vitro and in vivo, especially the differential expression of hub bridge genes. Indeed, as our project was based purely on bioinformatics, its predictions of interactions between hub genes should be validated in molecular experiments.
Future research should explore the role of HLA-A, HMOX1, JUN, endocytosis, CAMs, and phagosome signaling in models of post-ICH depression and in patients. Hopefully, this future work will clarify the underlying mechanism and highlight novel avenues for therapeutic intervention.r
We identified the hub bridge genes and signaling pathways related to post-ICH depression from a global, unbiased perspective, providing candidate molecules and functional pathways for further studies aimed at elucidating the pathogenesis of post-ICH depression.
This study received support from the National Natural Science Foundation of China (81860226), the Guangxi Natural Science Foundation (2018GXNSFAA294154), and the Guangxi Medical and Health Appropriate Technology Development and Application Project (S2018073).
The authors report no conflicts of interest in this work.
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